Canonical Allele Identifier: CA205703
Gene: CDKL5 HGNC NCBI

Linked Data

ClinVar Variation Id: 210644
dbSNP Id: rs747554139
gnomAD v2: X-18631334-C-T
gnomAD v3: X-18613214-C-T
gnomAD v4: X-18613214-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18613214C>T , CM000685.2:g.18613214C>T GRCh38
NC_000023.10:g.18631334C>T , CM000685.1:g.18631334C>T GRCh37
NC_000023.9:g.18541255C>T NCBI36
NG_008475.1:g.192610C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000623535.2:c.2215C>T MANE Select ENSP00000485244.1:p.Leu739=
ENST00000635828.1:c.2215C>T ENSP00000490170.1:p.Leu739=
ENST00000674046.1:c.2215C>T ENSP00000501174.1:p.Leu739=
ENST00000379989.6:c.2215C>T ENSP00000369325.3:p.Leu739=
ENST00000379996.7:c.2215C>T ENSP00000369332.3:p.Leu739=
ENST00000463994.4:c.2215C>T ENSP00000485184.1:p.Leu739=
ENST00000623535.1:c.2215C>T ENSP00000485244.1:p.Leu739=
NM_001037343.1:c.2215C>T NP_001032420.1:p.Leu739=
NM_003159.2:c.2215C>T NP_003150.1:p.Leu739=
XM_011545569.1:c.2164C>T XP_011543871.1:p.Leu722=
XM_011545570.1:c.2083C>T XP_011543872.1:p.Leu695=
XR_950484.1:n.2467C>T
NM_001323289.1:c.2215C>T NP_001310218.1:p.Leu739=
NM_001323289.2:c.2215C>T MANE Select NP_001310218.1:p.Leu739=
NM_001037343.2:c.2215C>T NP_001032420.1:p.Leu739=
NM_003159.3:c.2215C>T NP_003150.1:p.Leu739=